Nicholas Arpaia

Assistant Professor

Columbia University Irving Medical Center

United States

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About

Dr. Nicholas Arpaia is an Assistant Professor at Columbia University Irving Medical Center in the United States. His research primarily focuses on the interplay between regulatory T cells and tissue cell interactions in lung and liver repair, as well as the development of innovative immunotherapies for cancer treatment. Recent articles highlight his work on the role of amphiregulin in tissue repair and the engineering of bacteria for therapeutic applications in colorectal neoplasia.

Articles (19)

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2025

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2020

Collaborators (11)

Anjali Saqi

Columbia University

UNITED STATES

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Atsushi Sugimoto

Columbia University in the City of New York

UNITED STATES

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Tal Danino

Columbia University

UNITED STATES

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Moritz Peiseler

Charité - Universitätsmedizin Berlin

GERMANY

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Raghu Kalluri

Professor and Chairman

The University of Texas MD Anderson Cancer Center

UNITED STATES

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Meghna Komaranchath

Columbia University

UNITED STATES

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Tetsuhiro Harimoto

Columbia University

UNITED STATES

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Yoshinobu Saito

Assistant Professor

Osaka University

JAPAN

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Jongwon Im

Columbia University

UNITED STATES

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Samuel Asfaha

University of Western Ontario

CANADA

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Daniel Gray

Joint Division Head and Laboratory Head

Walter and Eliza Hall Institute of Medical Research

AUSTRALIA

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Nicholas Arpaia

Research Interests

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Articles (19)

Hepatic stellate cells control liver zonation, size and functions via R-spondin 3

Heparan sulfate regulates amphiregulin programming of tissue reparative lung mesenchymal cells during influenza A virus infection in mice

An amphiregulin reporter mouse enables transcriptional and clonal expansion analysis of reparative lung Tregs

Treg–tissue cell interactions in repair and regeneration

Programmable bacteria synergize with PD-1 blockade to overcome cancer cell–intrinsic immune resistance mechanisms

Amphiregulin from regulatory T cells promotes liver fibrosis and insulin resistance in non-alcoholic steatohepatitis.

Efficient Generation of Murine Chimeric Antigen Receptor (CAR)-T Cells.

Engineering tumor-colonizing E. coli Nissle 1917 for detection and treatment of colorectal neoplasia.

Regulation of the alveolar regenerative niche by amphiregulin-producing regulatory T cells

Dietary tryptophan deficiency promotes gut RORγt+ Treg cells at the expense of Gata3+ Treg cells and alters commensal microbiota metabolism

Probiotic-guided CAR-T cells for solid tumor targeting

Neo-Adjuvant immunotherapies: Bladder cancer as a platform for drug development targeting mucosal immunity.

Engineering bacteria as interactive cancer therapies

A programmable encapsulation system improves delivery of therapeutic bacteria in mice

The Origin and Contribution of Cancer-Associated Fibroblasts in Colorectal Carcinogenesis

CXCL13 shapes tertiary lymphoid structures and promotes response to immunotherapy in bladder cancer

Promotion of cholangiocarcinoma growth by diverse cancer-associated fibroblast subpopulations

Tumor restriction by type I collagen opposes tumor-promoting effects of cancer-associated fibroblasts

Engineered probiotics for local tumor delivery of checkpoint blockade nanobodies

Collaborators (11)

Anjali Saqi

Atsushi Sugimoto

Tal Danino

Moritz Peiseler

Raghu Kalluri

Meghna Komaranchath

Tetsuhiro Harimoto

Yoshinobu Saito

Jongwon Im

Samuel Asfaha

Daniel Gray

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